Fluorinated alcoholates

ABSTRACT

FLUORINATED ALCOHOLATES ARE PREPARED BY REACTING A FLUORO-KETONE WITH AN ALKALI METAL FLUORIDE. THE ALCOHOLATES MAY BE REACTED WITH ACYL HALIDES TO PRODUCE ESTERS USEFUL FOR ENHANCING THE WATER- AND OIL-REPELLENCY OF TEXTILES.

United States Patent 3,702,870 FLUORINATED ALCOHOLATES Allen G. Pittman, El Cerrito, and William L. Wasley, Berkeley, Calif., assignors to the United States of America as represented by the Secretary of Agriculture No Drawing. Application May 21, 1969, Ser. No. 826,655,

now Patent No. 3,637,791, which is a division of application Ser. No. 704,206, Dec. 28, 1967, now Patent No. 3,465,050, which is a division of application Ser. No. 623,483, Jan. 9, 1967, now Patent No. 3,419,602, which in turn is a division of application Ser. No. 398,129, Sept. 21, 1964, now Patent No. 3,384,628. Divided and this application July 9, 1971, Ser. No.

Int. Cl. C07c 35/02 U.S. Cl. 260-617 R 2 Claims ABSTRACT OF THE DISCLOSURE Fluorinated alcoholates are prepared by reacting a fluoro-ketone with an alkali metal fluoride. The alcoholates may be reacted with acyl halides to produce esters useful for enhancing the waterand oil-repellency of textiles.

This is a division of our co-pending application Ser. No. 826,655, filed May 21, 1969, now Pat. 3,637,791, which in turn is a division of Ser. No. 704,206, filed Dec. 28, 1967, now Pat. 3,465,050, which in turn is a division of Ser. No. 623,483, filed Jan. 9, 1967, now Pat. 3,419,602, which in turn is a division of Ser. No. 398,129, filed Sept. 21, 1964, now Pat. 3,384,628.

A non-exclusive, irrevocable, royalty-free license in the invention herein described, throughout the world for all purposes of the United States Government, with the power to grant sublicenses for such purposes, is hereby granted to the Government of the United States of America.

DESCRIPTION OF THE INVENTION Thus: I NaBHr (I; Acid halide C IO-H (wherein Ac is an acyl radical) It is to be particularly observed that the conventional procedure requires a reduction step and that the ester product contains a hydrogen atom on the alpha position of the alcohol moiety. (This hydrogen atom is indicated above by an asterisk.)

In accordance with the invention, fluorinated esters are prepared from ketones. In a first step, the ketone is reacted with an alkali metal fluoride to convert the carbonyl radical of the ketone into an alkali metal fluorocarbinolate radical, that is, a fiuorocarbinol group wherein the hydrogen of the hydroxyl radical is replaced by alkali metal. Thus:

3,702,870 Patented Nov. 14, 1972 ice 0=l MO-(IJ-F (M being an alkali metal) Then, the intermediate is reacted with an organic acid halide to form an ester, as follows:

It is evident from the above formulas that the key step in the synthesis is the reaction of the ketone with the alkali metal fluoride. This reaction not only changes the ketone function to an alcohol function without requiring use of a reducing agent, but also adds a fluorine group which carries over to the ester; that is, the ester contains a fluorine group on the alpha carbon atom of the alcohol moiety. This is an unusual type of structure which gives the products especially useful properties. For example, the products can be used to provide oiland watermepellent finishes on textiles and the repellency attained is substantially greater than that achieved with the corresponding compounds wherein the same position is occupied by hydrogen.

The process of the invention is by no means limited to the example above but is of great versatility and, generically, can be applied to any aliphatic open-chain or closed-chain) ketone which contains at least two fluorine groups adjacent to the carbonyl group. In other words, the carbon atoms connected to the carbonyl group must contain at least two fluorine atoms-distributed on these carbon atoms symmetrically or asymmetrically. These fluorine groups are a critical item to activate the carbonyl group so that it will undergo the desired transformation when contacted with the alkali metal fluoride. Especially good results are obtained when the carbon atoms adjacent to the carbonyl radical contain halogen radicals (i.e., F, Cl, Br, or I) in addition to the minimum of two fluorine groups. In this connection it may be noted that although halogens of higher atomic weight than fluorinei.e., Cl, Br, and I-are not effective by themselves to activate the carbonyl group, they can be employed to supplement the activating influence of fluorine groups. Beyond the positions adjacent to the carbonyl group, the structure of the ketone is of no criticality to the process and available sites may be occupied, for example, by hydrogen or halogen. In other words, the critical item for the process aspect of this invention is that the starting compound contain a carbonyl group activated by adjacent fluorine atoms as explained hereinabove; the remainder of the starting compound is not material to the process. Of course, this remainder may be limited in accordance with certain parameters to provide particular desired characteristics in the ester products. However, such limitation concerns the character of the ester product, not the operation of the process.

Typical examples of ketones to which the process of the invention may be applied and the corresponding ester 4 products are given below by way of illustration but not Wherein R represents an alkyl group containing 1 to 18 limitation: cabon atoms or a cycloalkyl group such as cyclopropyl,

cyclobutyl, or cyclohexyl.

Ester (product) (Ac is an acyl Wherein n is a number from 3 to 10 Compounds containing other halogen atoms in addition to fluorine (Y is Cl, Br, or I) wherein n is a number from 0 to 18 Compounds containing hydrogen in additiloirzi t108)fluorine (n and n are each a number from o It is also within the broad scope of the invention to utilize, as the starting material, ketones containing more than one carbonyl group. By adjustment of the proportions of reactants in line with usual stoichiometrical relationships, diesters are produced. Typical in this category are the following:

ing the solvent therefrom under vacuum. Where it is desired to produce an ester, the intermediate is not isolated but employed just as it is formed. The esterification is accomplished simply by adding the desired acid halide and stirring the mixture. The temperature is not critical and may range, for example, from 0 to C. No novelty is Generically, a preferred class of ketones which may be used in the process of the invention and the intermediates and the esters formed therefrom may be represented by the following structures:

Wherein each R represents a member of the group consisting of hydrogen, halogen, alkyl, haloalkyl, cycloalkyl, and halocycloalkyl and wherein at least two of the Rs are fluorine. Ac represents an acyl radical of an organic acid. M represents an alkali metal.

The fluorocarbin-olates and the esters responding to the structure given above in columns B and C are new compounds, not heretofore prepared or described.

As noted above, in the first step of the synthesis the fluoroketone is reacted with an alkali metal fluoride. As the latter reagent, potassium fluoride is generally preferred, but the fluorides of sodium, cesium, and rubidium may also be used. The reaction is generally conducted in an inert solvent for the 'ketone, for example, acetonitrile, dioxane, tetrahydrofuran, tetramethylene sulphone, diglyme (an abbreviated name for dimethyl ether of dicthylene glycol), etc. The alkali metal fluoride is only slightly soluble in these solvents and the disappearance of undispersed alkali metal fluoride during the reaction supplies a useful indication of formation of the desired intermediate (which is soluble). The temperature of reaction is not critical. Generally, temperatures over 35 C. are avoided to prevent decomposition of the intermediate. Usually, the reaction is conducted at room temperature for convenience but it does not take place at much lower temperatures. Where the starting ketone is a gas (for example, hexafluoroacetone) it is preferred to cool the system first to get the ketone into solution. Then, the temperature can be increased-for example, allowed to warm to room temperature-to accelerate the reaction. To prevent hydrolysis of the intermediate, the reaction is con ducted under anhydrous conditions. It is also helpful to remove air (which may contain moisture) 'by flushing the reaction vessel with dry, inert gas such as nitrogen. When the intermediate is formed-as evidenced by disappearance of undissolved alkali metal fluoride-the system is ready for further treatment. Where the intermediate (the fluorocarbinolate) is intended as the product, it is isolated from the reaction system by evaporatclaimed, per se, in this esterificatilon-it is analogous to conventional esterification by reacting an acid halide with an alcoholate.

The ester is recovered from the system by adding water and separating the organic phase from the aqueous phase containing dissolved alkali metal salt. The organic phase may then be dried and the product separated by distillation. In the alternative, the reaction mixture may be filtered to remove alkali metal salt and the product isolated by distillation.

In the esterification step, one can use any desired acid halide. Typically, the acid halide may be a carbonyl halide, a sulphonyl halide, or a haloformate. Compounds which may be used are listed below by way of illustration and not limitation:

Unsaturated acid halides, for example, compounds of the type:

CHF-t'l'l-X wherein X is F, Cl, Br, or I and R is H or a lower alkyl radical.

Saturated acid halides, for example, compounds of the type:

wherein X is F, Cl, Br, or I and Alk is an alkyl radical containing one to 18 carbon atoms.

Aromatic acid halides, for example, benzoyl, toluyl, xyloyl, naphthoyl, anisoyl, dodecylbenzoyl, parachlorobenzoyl, nitrobenzoyl, 2,4-dichlorobenzoyl, etc. fluorides, chlorides, bromides, or iodides.

Fluorinated acid halides, for example, compounds of the type:

wherein X is F, Cl, Br, or I and n has a value from 0 to 18.

Other carbonyl halides such as phenylacetyl chloride, ethoxyacetyl chloride, crotonyl chloride, hexahydrobenzoyl chloride, nitrobenzoyl chloride, acetyl-benzoyl chloride, oleoyl chloride, linoleoyl chloride, chloroacetyl chloride, cinnamyl chloride, phenoxyacetyl chloride, etc.

Aromatic sulphonyl halides, for example, benzene, toluene, xylene, naphthalene, anisole, phenetole, dodecylbenzene, nitrobenzene, parachlorobenzene, 2,4-dichlorobenzene, wtoluene, etc. sulphonyl fluorides, chlorides, bromides, or iodides.

Saturated aliphatic sulphonyl halides, for example, compounds of the type:

wherein X is F, Cl, Br, or I and n has a value from to 18.

Fluorinated aliphatic sulphonyl halides, for example, compounds of the type:

wherein X is F, Cl, Br, or I and n has a value from O to 1'8.

Unsaturated sulphonyl halides, for example, compounds of the type:

wherein X is F, Cl, Br or I and R is H or a lower alkyl group.

Other sulphonyl halides, for example, cyclohexane sulphonyl chloride, benzyl sulphonyl chloride, etc.

Saturated haloformatcs, for example, compounds of the type:

i AlkO-( JX wherein X is F, Cl, Br, or I and Alk is an alkyl radical containing one to 18 carbon atoms.

Aromatic haloformates, for example, compounds of the type:

i Ar-O-(lX wherein X is F, Cl, Br or I and Ar is an aryl radical such as phenyl, tolyl, xylyl, naphthyl, etc.

Fluorinated haloformates, for example, compounds of the types:

O CF3--(C F. ..-oH2-o-i :-X

wherein X is F, Cl, Br or I and n has a value from 0 to 18. Unsaturated haloformates, typically compounds of the types:

wherein X is F, Cl, Br, or I and R is H or a lower alkyl radical.

Although it is generally preferred to utilize monofunctional acid halides in the esterification, it is within the broad ambit of the invention to use polyfunctional agents, for example, maleyl chloride, malonyl chloride, succinyl chloride, adipyl chloride, itaconyl chloride, benzene disulphonyl chloride, ethylene glycol bis-chloroformate, diethylene glycol bis-chloroformate, the bischloroformate of 2,2-bis-(parahydroxyphenyl)propane, and the like. Where polyfunctional acid halides are employed, the proportions of the acid halide and the above-described intermediate may be selected to attain complete or partial esterification of the available acid halide sites.

The alkali metal fiuorocarbinolates produced in accordance with the invention are primarily useful as intermediates for the preparation of esters as herein disclosed.

The esters produced in accordance with the invention may be used in many areas wherein esters in general are employed, i.e., as lubricants, plasticizers, and hydraulic fluids. Moreover, because of their content of fluorine, particularly the fluorine atom on the u-carbon atom of the alcohol moiety, they are useful in such applications as oil and water repellents. Thus, by applying solutions of these esters to materials such as paper, fabrics, yarns, etc.,

these materials will resist the penetration of oils and water. Of particular utility are the esters derived from acrylic, methacrylic, or other acids containing a CH =C group. These esters are polymerizable and can be formed into homopolymers or copolymers by conventional polymerization techniques as, for example, heating at about -85 C. in the presence of a small proportion of a polymerization initiator such as a,a'-azobisisobutyronitrile. These novel polymers can be used in such applications as coating and as adhesives in laminating sheet materials. Of especial interest is that the polymers exhibit low solubility in common solvents such as benzene, toluene, xylene, etc., whereas they are soluble in fluorinated solvents such as benzotrifiuoride, 1,3-bis-trifluoromethyl benzene, and the like. Thus, the polymers in question can be used in coating and adhesive applications where other polymeric materials are unsuitable because of solubility in common organic solvents.

A particular phase of the present invention is concerned with the treatment of fibrous materials, such as textiles, in order to improve their properties, e.g., to improve their oiland water-repellency. In applying this phase of the invention, an ester derived from acrylic acid, methacrylic acid, or other organic acid containing a CH =C group is prepared as hereinabove described. This polymerizable ester is then applied to the fibrous material, using either of two procedures. In one procedue the monomeric ester is applied to the fibrous material and polymerized in situ thereon by applying ionizing radiation, a persulphate, a peroxide, an azo polymerization initiator, or a redox catalyst system (typically, a combination of a reducing agent such as hydrazine sulfate, ferrous sulphate, sodium bisulphite, etc., and an oxidizing agent such as hydrogen peroxide, benzoyl peroxide, sodium peracetate, etc.). In the preferred procedure, the polymerizable ester is first formed into a polymer and then applied to the fibrous material. The polymer may be a homopolymer, that is, one consisting of recurring units of the ester, or it may be a copolymer, that is, a polymer containing recurring units of the ester interspersed with units derived from a different vinyl monomer, such as ethylene, propylene, styrene, vinyl chloride, acrylonitrile, methyl methacrylate or acrylate, acrylamide, mathacrylamide, vinyl acetate or stearate, butadiene, and the like. The polymers are prepared by conventional techniques. For example, the polymerizable ester per se or admixed with a different vinyl monomer is heated at about 70-85 C. in the presence of a small proportion of a polymerization initiator such as a,a'-azobisisobutyronitrile. As illustrative examples of this procedure, when heptafiuoroisopropyl acrylate is formed into a homopolymer, the product will be a polymer containing in its skeletal chain recurring units of the structure:

CF:-( 3FCFa In the event that the same ester is copolymerized with butyl acrylate, for example, the copolymer product will contain in its skeletal chain recurring units of the above type plus recurring units derived from butyl acrylate, i.e.

In any event, the polymers (homoor co-polymers) are applied to the fibrous material in conventional manner. Typically, the polymer is dissolved in an inert, volatile solvent-for example, benzotrifiuoride or 1,3-bis-trifiuorobenzene-and the resulting solution applied to the fibrous material by a conventional dip and pad technique. By varying the concentration of polymer in solution and the degree of padding, the amount of polymer deposited on the material may be varied. Typically, the amount of polymer may be about from 0.1 to 20%, based on the weight of fibrous material but it is obvious that higher or lower proportions can be used if desired. Usually, in treating textiles such as fabrics the amount of polymer is limited to about 0.1 to 10% to attain the desired repellency improvement without interference with the hand of the textile. Generally, it is preferred to subject the fibrous material to a conventional curing operation after application of the polymer solution thereto in order to bond the polymer to the fibers. As an example of such treatment, the fibrous material is heated in the range of about 50 to 150 C. for a period of about to 30 minutes. The solvent (from the polymer solution) may be evaporated in a separate step prior to curing or may be simply evaporated during the curing operation. Fibrous materials treated with the polymers of the invention display an increased resistance to becoming soiled because they repel both Waterand oil-borne soils and stains. Moreover, the improvements so rendered are durable-they are retained despite laundering and dry-cleaning of the product.

The invention may be utilized for improving the properties of all types of fibrous materials, for example, paper, cotton; linen; hemp; jute; ramie; sisal; cellulose acetate rayons; cellulose acetate-butyrate rayons; saponified acetate rayons; viscose rayons; cuprammoniurn rayons; ethyl cellulose; fibers prepared from amylase, algins, or pectins; wool; silk; animal hair; mohair; leather; fur; regenerated protein fibers prepared from casein, soybean, peanut pro teins, zein, gluten, egg albumin, collagen, or keratins; nylon; polyurethane fibers; polyester fibers such as polyethylene terephthalate; polyacrylonitrile-based fibers; or fibers of inorganic origin such as asbestos, glass, etc. The invention may be applied to textile materials which are in the form of bulk fibers, filaments, yarns, threads, slivers, roving, top, webbing, cord, tape, woven or knitted fabrics, felts or other non-woven fabrics, garments or garment parts.

Included in the invention is the process which comprises reacting a ketone of the structure wherein n is a number from 3 to 10, with an alkali metal fluoride to produce an intermediate of the structure wherein n is as defined above and M is an alkali metal, and reacting said intermediate with an organic acid halide to produce an ester of the structure Art-O- F (CF91:

wherein Ac is the acyl radical of an organic acid and n is as defined above.

EXAMPLES The invention is further demonstrated by the following illustrative examples. The various tests described in the examples were carried out as described below:'

Oil Repellency: The 3M oil repellency test described by Grajeck and Peterson, Textile Research Journal, 32, pages 320-331, 1962. Ratings are from O to 150, with the higher values signifying the greater resistance to oil penetration.

Water Repellency: AATC spray test, method 22-1952. Ratings are from 0 to 100 with the higher values signifying greater resistance to water penetration.

Home Laundering Procedure: An agitator-type home washing machine was operated under the following conditions: Low water level (about 11 gal.); wash temperature, 115-125 F.; rinse temperature, 95-115 F.; normal agitation; 12-minute wash cycle; load--2 pounds ballast plus samples, total weight not exceeding 4 pounds; 100

cc. Tide detergent. Washed samples were dried 15 minutes in a forced draft oven at 160 F.

EXAMPLE 1 Preparation of heptafluoroisopropyl acrylates O C F; CHz=CHi J--O (J F An apparatus was assembled including a S-neck flask equipped with thermometer, stirrer, and a reflux condenser cooled with Dry Ice (solid CO The open end of the condenser was connected to a drying tube to prevent ingress of moisture from the air. The system was flushed with nitrogen, then 76 g. (0.5 mole) dry cesium fluoride and 200 ml. dry diglyme were placed in the flask and mixed. The dispersion was cooled to minus 40 C. by applying a Dry-Ice cooling bath to the flask, and 84 grams (0.506 mole) of hexafluoroacetone was introduced into the flask. The cooling bath was then removed and the system allowed to come to room temperature. As the system warmed, formation of the fluorocarbinolate intermediate was evidenced by disappearance of the dispersed CsF, giving a homogeneous solution.

Acryloyl chloride (41 g., 0.45 mole) was then added with stirring. A precipitate formed immediately. Stirring was continued at room temperature for /2 hour.

The mixture was poured into 3 volumes of water. The lower phase was collected, washed three times with 100- ml. portions of water. Eighty-six grams of crude product was obtained. The product was dried over calcium sulphate, and distilled in vacuo through a short Vigreux column. Seventy-eight grams of purified product-heptafluoroisopropyl acrylate-was collected as a clear liquid, B.P.. 75.5 C. at 760 mm. of Hg. Calculated for CsFqHgOz (percent): C, 29.99; F, 55.5; H, 1.25. Found (percent): C, 29.42; F, 56.2; H, 1.77.

EXAMPLE 2 Preparation of polymer of heptafiuoroisopropyl acrylate Preparation of heptafluoroisopropyl methacrylate The procedure of Example 1 was repeated, using methacryloyl chloride in place of acryloyl chloride. A 70% yield of heptafiuoroisopropyl methacrylate was obtained as a clear liquid, B.P. 85-86 C. at 760 mm.

EXAMPLE 4 Preparation of polymer of heptafluoroisopropyl methacrylate A 4-gram sample of the ester prepared in Example 3 and mg. of a,dazobisisobutyronitrile were heated at 78 C. for 3 hours in a sealed vessel. The polymer was a glassy, brittle resin, soluble in benzotrifluoride and 1,3- bis-trifluoromethyl benzene.

EXAMPLE 5 Preparation of heptafluoroisopropyl acetate The procedure of Example 1 was followed, substituting acetyl bromide for the acryloyl chloride. The amounts of material used were:

Cesium fluoride: 40 g., 0.26 mole Hexafluoroacetone: 44 g., 0.26 mole Diglyme (solvent): 100 ml.

Acetyl bromide: 19.6 ml., 0.26 mole The product, heptafiuoroisopropyl acetate, was obtained as a clear liquid in a yield of 32 grams, B.P. 65-66 C. at 760 mm. Hg.

EXAMPLE 6 Preparation of heptafluoroisopropyl propionate OF: H I GHaCH2-O-O F The procedure of Example 1 was repeated, using the following materials:

Potassium fluoride: 6.6 g., 0.114 mole Diglyme (solvent): 50 ml. Hexafiuoroacetone: 18.8 g., 0.113 mole l Propionyl chloride: 9 ml., 0.113 mole The product, heptafluoroisopropyl propionate, was obtained in a yield of 35% as a clear liquid, B.P. 83-84 C. at 760 mm. Hg.

EXAMPLE 7 Preparation of fl-chloro-hexafluoroisopropyl acrylate EXAMPLE 8 Polymer of fl-chloro-hexafluoroisopropyl acrylate A 3-gram sample of the acrylate prepared in Example 7 and 50 mg. of a,a'-azobisisobutyronitrile were heated at 78 C. for 3 hours in a sealed vessel. The polymer was a glassy solid which softened at about 85 C. and which was soluble in benzotrifluoride and 1,3-bis-trifluoromethyl benzene.

EXAMPLE 9 Preparation of ,8-chloro-hexafluoroisopropyl methacrylate The procedure of Example 7 was repeated, substituting the equivalent amount of methacryloyl chloride for the acryloyl chloride.

The ester product was recovered in a yield of 32 grams, B.P. 123-124 C. at 760 mm. Hg.

EXAMPLE 10 Polymer of B-chloro-hexafluoroisopropyl methacrylate A 4-gram sample of the ester prepared in Example 9 and 100 mg. of a,eU-azobisisobutyronitrile were heated at 78 C. for 3 hours in a sealed vessel. The polymer was a glassy, brittle solid which softened at about 100 C. It was soluble in benzotrifluoride and 1,3-bis-trifluoromethyl benzene.

12 EXAMPLE 11 Preparation of fl,[3'-dichloro-pentafluoroisopropyl methacrylate Cesium fluoride (30.4 g., 0.2 mole) was dispersed in 100 ml. diglyme and the dispersion was cooled to 0 C. 1,3- dichlorotetrafluoroacetone (40 g., 0.2 mole) was added with stirring and the mixture allowed to warm to room temperature. After the mixture had cleared, 20 g. of methacryloyl chloride was added and stirring was continued for /2 hour at room temperature.

The mixture was poured into 3 volumes of water and the lower layer separated, washed with water, dried, and distilled, giving a 32% yield (18 g.) of ,8,fi-dichloro-pentafluoroisopropyl methacrylate, B.P. 156-157 C. at 760 mm. Hg.

EXAMPLE 12 Polymer of 5,18-dichloro-pentafluoroisopropyl methacrylate A 4-gram sample of the ester prepared in Example 11 and 75 mg. of a,a-azobisisobutyronitrile were heated at C. for 4 hours in a sealed vessel. The polymer was a hard, brittle solid. It was soluble in benzotrifluoride and 1,3-bis-trifluoromethyl benzene.

EXAMPLE 13 Preparation of 5,,8'-dichloro-pentafluoroisopropyl acrylate The procedure of Example 11 was repeated, substituting the equivalent amount of acryloyl chloride for the methacryloyl chloride. The ester product Was obtained in a yield of 32 grams, B.P. 145.5 C. at 760 mm. Hg.

EXAMPLE 14 Polymer of p,B'-di-chloro-pentafluoroisopropyl acrylate A 4-gram sample of the ester prepared in Example 13 and 75 mg. of a,a'-azobisisobutyronitrile were heated at 80 C. for 4 hours in a sealed vessel. The polymer was an amorphous, clear solid. It was soluble in benzotrifluoride and 1,3-bistrifluoromethyl benzene.

EXAMPLE 15 Preparation of acrylic acid ester of perfluoroheptan-4-o1 Cesium fluoride (10.9 g. 0.072 mole) was dispersed in 50 ml. diglyme and the dispersion cooled to 0 C. Perfiuoroheptanl-one (26.5 g., 0.072 mole) was added with stirring. After formation of the intermediate, 6.48 g. of acryloyl chloride was added and stirring was continued for /2 hour at room temperature.

The mixture was poured in 3 volumes of water and the lower layer separated, washed with water, dried, and distilled. The product, having the formula given above, was obtained in a 30-gram yield, B.P. 167 C. at 760 mm. Hg.

The product was polymerized in the following manner:

A 4-gram sample of the acrylate and 75 mg. of egosazobisisobutyronitrile were heated at 80 C. for 4 hours in a sealed vessel. The polymer was a glassy, amorphous solid. It was soluble in benzotrifluoride and 1,3-bis-trifluoromethyl benzene.

EXAMPLE 16 Preparation of fl-chloro-hexafluoroisopropyl benzenesulphonate Using the procedure described in Example 1, the following materials were applied to the reaction:

Cesium fluoride: 37 grams Diglyme (solvent): 100 ml. Monochloro-pentafluoroacetone: 45 grams Benzene sulphonyl chloride: 30.4 cc.

The product was obtained in a yield of 45 grams, B.P. about 240 C. at 7-60 mm. Hg.

EXAMPLE 17 10 (A) Preparation of CH; 0 CF, CHz=$--( J OCH2CHr-O -OJJ F Using the procedure of Example 1, the following materials were applied to the reaction:

Potassium fluoride: 1.7 grams Diglyme (solvent): 25 ml.

Hexafiuoroacetone: 5 grams Chloroformate of ethylene glycol mono-methacrylate:

CHI 0 O EXAMPLE 18 Oiland water-repellency of polyacrylates Polymers prepared as described above were dissolved in trifluoromethyl benzene. Solutions ranging in concentration from /2 to 8% were prepared for each polymer. These solutions were then applied to samples of wool fabric by the following method:

The cloth was immersed in the solution to thoroughly wet the cloth with the liquid. Then, the cloth was passed through squeeze rolls to provide a wet pick-up of about 100%. The treated fabric was then cured in a forced-draft oven at 110 C. for 20 minutes. After curing, the samples were weighed to determine the amount of polymer on the fabric.

The fabric samples were then subiected to tests for oiland water-repellency. The results are tabulated below:

OIL- AND WATER-REPELLENCY TESTS Control (untreated W001) It is evident from the above data that all the polymers provided good Water repellency. With regard to oil repellency, the polymer of heptafluoroisopropyl acrylate provided the best results, whereas replacement of two fluorine groups by chlorine vitiated the oil-repellent character.

EXAMPLE 19 Durability to laundering of poly-heptafluoroisopropyl acrylate 'Ihe wool samples treated with poly-heptafluoroisopropyl acrylate as described in Example 18 were tested for oiland water-repellency as initially prepared and after repeated Washing by the home laundering procedure described hereinabove. The results are tabulated below:

Oil repelleney Water repellenoy After 3 After 6 After 3 After 6 Welght 1 Initial washes washes Initial washes washes 6.6 110 110 110 100 100 100 1.6 100 90 90 100 100 100 0.8 100 60 100 100 None (control)- 0 50-60 l Polyheptafluoroisopropyl acrylate on fabric, percent.

EXAMPLE 2.0

Water repellency of poly-methacrylates Samples of wool cloth were treated with solutions of polymethacrylates as described above in Example 18. The water repellency of the products is tabulated below:

WATER-REPELLENCY TESTS Weight of polymer on fabric, Water R percent repellency -CF(CF:): 5.6 --CFCFs)| 1.4 100 --CF CFz): 0.35 100 (IJFI 7. 0 100 Same as above 2. 0 100 D0 1. 0 100 --CF(CF:C1): 5.0 100 -GF(C F101): 1.3 100 CF(GF:C1): 0.6 100 Control (untreated) 0 60-60 EXAMPLE 21 Oiland Water-Repellency of CH: 3 (I? C F; Polymer of CHz=( J--C-0CHzCHaO-CO--F The polymer solution prepared as described in Example 17, part B, was diluted further with benzotrifiuoride to prepare solutions at several different polymer concentrations. These solutions were applied to wool cloth by immersing the cloth in the solution, pressing to about 100% wet pick-up and curing in an oven at C. for 20 minutes. The results of oiland water-repellency tests on the products are tabulated. below:

15 EXAMPLE 22 In situ polymerization of heptafluoroisopropyl acrylate on wool A swatch of wool flannel was immersed in a 0.2% aqueous solution of ferrous sulphate, squeezed, and dried. The wool was then immersed for one hour in a solution (at 95100 C.) containing 200 ml. water, 10 ml. heptafiuoroisopropyl acrylate, and 0.03% hydrogen peroxide. The swatch was then washed in water, dried, and weighed to determine the polymer uptake. In this case the fabric had a 20% increase in weight.

'EXAMPLE 23 Co-polymerization of heptafluoroisopropyl acrylate with n-butyl acrylate Into a 4-02. screw top vial were placed EXAMPLE 24 Preparation and isolation of cesium heptafluoroisopropylate (IJF:

Into a dry, 3-neck, round-bottom flask with attached Dry-Ice condenser Were placed 17.4 g. cesium fluoride and 25 cc. tetrahydrofuran. The dispersion was stirred, cooled in an ice bath (about 5 C.), and 19 g. of hexaliuoroacetone was introduced. After about minutes the alcoholate had formed as evidenced by the disappearance of C F. The flask was then connected to a vacuum system and the tetrahydrofuran was removed at room temperature under 0.1 mm. vacuum. The white, powdery, solid product (cesium heptafluoroisopropylate) remained. Unlike many alcoholates, it did not appear to be hygroscopic.- It was soluble in such solvents as acetone, :N,N-dimethylformamide, and diglyme but insoluble in such non-polar solvents as n-heptane and chloroform. It appeared to be thermally stable up to about 90 l00 C. At higher temperatures it melted with decomposition, evolving hexafiuoroacetone.

Having thus described the invention, we claim:

1. The process which comprises reacting a ketone of the structure where n is a number from 3 to 10, with an alkali metal fluoride under anhydrous conditions at a temperature up to about C. in a system wherein the sole reactants are the said ketone and alkali metal fluoride, to produce an alkali metal fluorocarbinolate of the structure MO- F (01%)..

kJ wherein M is an alkali metal and n is as defined above, and recovering said alkali metal :fluorocarbinolate.

2. An alkali metal fluorocarbinolate of the structure wherein M is an alkali metal and n is a number from 3 to 10.

References Cited UNITED STATES PATENTS 3,274,239 9/1966 Selman 26O'--514 3,317,616 5/1967 Weinmayr 260-633 3,384,628 5/1968 Pittman et a1. 260-895 HOWARD T. MARS, Primary Examiner 

